<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Pieterse, Corné M. J.</dc:creator>
  <dc:creator>Pelt, Johan A. van</dc:creator>
  <dc:creator>Ton, Jurriaan</dc:creator>
  <dc:creator>Parchmann, Stefanie</dc:creator>
  <dc:creator>Mueller, Martin J.</dc:creator>
  <dc:creator>Buchala, Antony J.</dc:creator>
  <dc:creator>Métraux, Jean-Pierre</dc:creator>
  <dc:creator>Loon, Leendert C. van</dc:creator>
  <dc:date>2000</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Plants develop an enhanced defensive capacity against a broad spectrum of plant  pathogens after colonization of the roots by selected strains of nonpathogenic  biocontrol bacteria. In &lt;i&gt;Arabidopsis thaliana&lt;/i&gt;, this induced systemic resistance  (ISR) functions independently of salicylic acid but requires an intact response to the  plant hormones jasmonic acid (JA) and ethylene. To further investigate the roles of JA  and ethylene in the ISR signalling pathway, the levels of these signalling molecules  were determined in &lt;i&gt;A. thaliana&lt;/i&gt; upon induction of ISR by &lt;i&gt;Pseudomonas  fluorescens&lt;/i&gt; WCS417r and subsequent challenge inoculation with  &lt;i&gt;Pseudomonas syringae&lt;/i&gt; pv. &lt;i&gt;tomato&lt;/i&gt; DC3000. Upon treatment of the roots  with ISR-inducing WCS417r bacteria, neither the JA content, nor the level of ethylene  evolution was altered in systemically resistant leaves. Infiltration of leaves with  WCS417r triggered the JA- and ethylene-dependent ISR pathway, but did not cause  local changes in the production of either of these signalling molecules. These results  indicate that rhizobacteria-mediated ISR is not based on the induction of changes in  the biosynthesis of either JA or ethylene. However, in ISR-expressing plants the  capacity to convert 1-aminocyclopropane-1-carboxylate (ACC) to ethylene was  significantly enhanced, providing a greater potential to produce ethylene upon  pathogen attack.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/300130</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/300130/files/1_metraux_rmi.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1006/pmpp.2000.0291</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Physiological and Molecular Plant Pathology. - 2000, vol. 57, no. 3, p. 123-134</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Rhizobacteria-mediated induced systemic resistance (ISR) in Arabidopsis requires sensitivity to jasmonate and ethylene but is not accompanied by an increase in their production</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
